# Zhejiang Hisoar Pharmaceutical Co. Ltd. - Inspection Records

Source: https://www.keypedia.com/companies/zhejiang-hisoar-pharmaceutical-co-ltd/ba703e0d-38b9-4058-8c78-88e0a083063f

> Inspection records and compliance data for Zhejiang Hisoar Pharmaceutical Co. Ltd. in Taizhou, None. Access full analysis and detailed observations.

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## Details

- Name: Zhejiang Hisoar Pharmaceutical Co. Ltd.
- FEI Number: 3003735151
- City: Taizhou
- State: None
- Country Name: China
- Address Line 1: 100 Waisha Branch Road, Jiaojiang
- Zip Code: None
- Business Operations: API MANUFACTURE, FDF MANUFACTURE

## Related Documents

- [FDA Inspection 1048535 - Zhejiang Hisoar Pharmaceutical Co. Ltd. - 2018-03-09](https://www.keypedia.com/records/fda_inspections/zhejiang-hisoar-pharmaceutical-co-ltd/d0941bf5-ceb4-4571-b81c-1614c12488b7) — classification: Voluntary Action Indicated (VAI), source: FDA, date: March 9, 2018
- [FDA Inspection 938356 - Zhejiang Hisoar Pharmaceutical Co. Ltd. - 2015-08-13](https://www.keypedia.com/records/fda_inspections/zhejiang-hisoar-pharmaceutical-co-ltd/68d9d139-2afa-41c8-9765-13f5c16eccd2) — classification: Official Action Indicated (OAI), source: FDA, date: August 13, 2015
- [FDA Inspection 938356 - Zhejiang Hisoar Pharmaceutical Co. Ltd. - 2015-08-13](https://www.keypedia.com/records/fda_inspections/zhejiang-hisoar-pharmaceutical-co-ltd/964f1299-6a28-4ded-a358-0f9a23b4de59) — classification: Official Action Indicated (OAI), source: FDA, date: August 13, 2015
- [FDA Inspection 819284 - Zhejiang Hisoar Pharmaceutical Co. Ltd. - 2013-01-18](https://www.keypedia.com/records/fda_inspections/zhejiang-hisoar-pharmaceutical-co-ltd/b90124bf-4b7f-430e-8b91-4bd3cf28b995) — classification: Voluntary Action Indicated (VAI), source: FDA, date: January 18, 2013
- [FDA Inspection 610604 - Zhejiang Hisoar Pharmaceutical Co. Ltd. - 2009-08-29](https://www.keypedia.com/records/fda_inspections/zhejiang-hisoar-pharmaceutical-co-ltd/91731218-eafc-4d22-b50d-c4becb406aa4) — classification: Voluntary Action Indicated (VAI), source: FDA, date: August 29, 2009

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